RecallHawk
Class I Recall

Andersen & Sons Shelling, Inc. Macadamia Nuts, Dry Roasted Style 6 25 lbs.

Andersen & Sons Shelling, Inc.

Summary

The FDA issued a Class I for Andersen & Sons Shelling, Inc. Macadamia Nuts, Dry Roasted Style 6 25 lbs. by Andersen & Sons Shelling, Inc.. Reason: Listeria monocytogenes contamination.

Details

Source

Food Recall

External ID

F-1389-2024

Action Date

2024-07-03

Status

Terminated

Category

food

Product Description

Andersen & Sons Shelling, Inc. Macadamia Nuts, Dry Roasted Style 6 25 lbs.

Lot/Code Info: lot code 26950-1-2-1 Expiration date: 4/12/2025

Quantity Affected: 2,850 lbs.

Reason for Recall

Listeria monocytogenes contamination

Distribution

U.S. distribution: ID No foreign distribution.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-05-16

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 58 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Andersen & Sons Shelling, Inc. has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Andersen & Sons Shelling, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Andersen & Sons Shelling, Inc. have FDA actions?

Andersen & Sons Shelling, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1389-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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